Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58273631C= , CM000679.2:g.58273631C= | GRCh38 |
| NC_000017.10:g.56350992C= , CM000679.1:g.56350992C= | GRCh37 |
| NC_000017.9:g.53705991C= | NCBI36 |
| NG_009629.1:g.12305G= , LRG_84:g.12305G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000578493.2:n.737G= | ||
| ENST00000699291.1:c.529G= | ENSP00000514272.1:p.Ala177= | |
| ENST00000699292.1:n.444G= | ||
| ENST00000225275.4:c.1404G= MANE Select | ENSP00000225275.3:p.Gly468= | |
| ENST00000225275.3:c.1404G= | ENSP00000225275.3:p.Gly468= | |
| NM_000250.1:c.1404G= , LRG_84t1:c.1404G= | NP_000241.1:p.Gly468= | |
| XM_011524821.1:c.1590G= | XP_011523123.1:p.Gly530= | |
| XM_011524822.1:c.1119G= | XP_011523124.1:p.Gly373= | |
| XM_011524823.1:c.1429G= | XP_011523125.1:p.Ala477= | |
| NM_000250.2:c.1404G= MANE Select | NP_000241.1:p.Gly468= |